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Barrington James

Senior Pharmacovigilance Licensing Manager

London
Posted 1 day ago
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Senior Pharmacovigilance Licensing Manager

Senior PV Licensing Manager

Seeking a Senior PV Licensing Manager with responsibility to manage the end-to-end process of developing and implementing Pharmacovigilance agreements.

Key Responsibilities

  • Collaborating with partners that delivers compliance and efficiency for both parties.
  • Collaborate with Global functions providing advice and support for commercial agreements.
  • Oversee and manage pharmacovigilance collaborations and alliances with external business partners.
  • Represent the PVA team in internal and external meetings whilst ensuring that PVA is effectively implemented and maintained.
  • Support audits and inspections related to pharmacovigilance collaborations.
  • Train and educate internal teams on pharmacovigilance standards and procedures.

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I’m in my final year doing Economics and I don’t know whether to apply for grad schemes now or do a masters first. What do you think?

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Also worth knowing: most autumn 2026 applications are open now. Timing matters more than you think.

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Graduate Consultant — 2026 Scheme

PwC·London, UK
£35,000/yr

Why you're a good match

Strong

Your economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.

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Why you're a good match

You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.

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Experience fit

Your summer at the bank plus your econometrics coursework map directly to the day-one responsibilities on this scheme — client modelling, market briefings, and deal support.

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Required experience:

  • Bachelor's degree preferably in Life Sciences.
  • Minimum of 5 years of experience in the pharmaceutical industry.
  • At least 3 years of specific experience in managing patient safety.
  • Strong understanding of global and local pharmacovigilance regulations and guidelines.
  • Proven ability to work effectively in cross-functional and international teams.

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Why apply?

  • Strong reputation as a specialist biopharmaceutical company.
  • Opportunity to make a meaningful impact on patients with high unmet medical needs.
  • Global organisation with an international pharmacovigilance and drug safety environment.
  • Exposure to innovative biologics and advanced therapies.

FTE (full time equivalent) - four months (potential to extend)

Remote work - Europe based wanted

Start date: ASAP

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Skills

Pharmacovigilance
Patient Safety
Compliance
Collaboration
Audits
Inspections
Training
Regulations
Guidelines
Cross-Functional Teams
Global Functions
Commercial Agreements
Pharmaceutical Industry
Biopharmaceutical
Drug Safety
Innovative Biologics

Location

London, England, United Kingdom

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